Canonical Allele Identifier: PA2827926911
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 219823
ClinVar RCV Id: RCV001018501 RCV001370713
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro103Ala
CA348715
NM_001354723.2:c.307C>G